USP53
Cancer Mutation
SNP
mRNA Expression
DNA & RNA Element
PPI
Disease
PTM
DNA Methylation
Proteomics
GWASdb
Disease associated variation - GWASdb
Chr
Pos
SNP ID(dbSNP 142)
Ref
Alt
Ori SNP ID
P-value
Drug Name
Drug Anno
GWAS Trait
HPO ID
DO ID
AA
Type
Trait or Drug
4
120151012
rs9996382
A
G
rs9996382
1.81E-04
Type 2 diabetes
HPOID:0005978
DOID:9352
G
intron
GWASdb_trait
4
120151452
rs10031033
T
C
rs10031033
2.85E-04
Type 2 diabetes
HPOID:0005978
DOID:9352
T
intron
GWASdb_trait
4
120159334
rs11944880
C
T
rs11944880
5.41E-04
Multiple complex diseases
HPOID:0000118
NA
C
intron
GWASdb_trait
4
120167111
rs7356185
T
C
rs7356185
0.000141
Coronary artery disease
HPOID:0001677
DOID:3393
C
intron
GWASdb_trait
4
120187611
rs11098499
C
T
rs11098499
9.00E-06
Corneal astigmatism
HPOID:0000483
DOID:10124
C
intron
GWASdb_trait
4
120214030
rs3749591
T
G
rs3749591
9.85E-04
Glycosylated haemoglobin levels
HPOID:0011902|HPOID:0000077|HPOID:0001626|HPOID:0000819|HPOID:0000479
DOID:1287|DOID:9351|DOID:557|DOID:5679
T
missense
GWASdb_trait